loading...| Preferred Name |
PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR 1 |
| Synonyms |
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, AND DEVELOPMENTAL DELAY |
| ID |
http://purl.bioontology.org/ontology/OMIM/176310 |
| altLabel |
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, AND DEVELOPMENTAL DELAY CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY PBXP1 PBX1/E2A FUSION GENE PBX1 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH HEARING LOSS, ABNORMAL EARS, AND DEVELOPMENTAL DELAY PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR PSEUDOGENE 1 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITHOUT HEARING LOSS, WITH OR WITHOUT ABNORMAL EARS OR DEVELOPMENTAL DELAY CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITHOUT HEARING LOSS OR ABNORMAL EARS, WITH DEVELOPMENTAL DELAY |
| cui |
C1418285 C4693972 C4693971 C4539968 C4693973 C2239801 C1867800 C4540544 |
| Gene Locus |
1q23 |
| Gene Symbol |
PBX1 CAKUHED |
| Has allelic variant |
http://purl.bioontology.org/ontology/OMIM/176310.0007 http://purl.bioontology.org/ontology/OMIM/176310.0002 http://purl.bioontology.org/ontology/OMIM/176310.0003 http://purl.bioontology.org/ontology/OMIM/176310.0004 http://purl.bioontology.org/ontology/OMIM/176310.0001 |
| MIMTYPEMEANING |
Gene with known sequence |
| Moved from |
600213 |
| notation |
176310 |
| OMIM Entry Type |
1 |
| OMIM MimType Value |
star |
| prefLabel |
PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR 1 |
| tui |
T028 T019 T047 |